Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Kitchen Utensils


sleer

Recommended Posts

sleer Contributor

We have a shared kitchen. It hasn't been a terrible issue yet. My husband is very cautious. I'm replacing our kitchen utensils (spatulas, etc) and wanted to know if there was a material that would be more resistent to cross contamination problems. I think I read that wood utensils were a no-go? How about silicon? Obviously they would be washed in the dishwasher between uses. Any thoughts?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



StephanieL Enthusiast

I prefer stainless single piece construction. This way there is no place for "gunk" to hid in.

Strawberry-Jam Enthusiast

silicone, metal, and plastic are all okay, imho. Be careful with plastics that get easily scratched, however.

wooden utensils and all cutting boards and colanders, regardless of construction, should be dedicated gluten-free only.

  • 2 months later...
ColbyCorey Newbie

I would also suggest silicone because of it's non-porous characteristic which doesn't retain odors or colors when you use it for stirring deep-colored food like tomato-based food products. They can be easily clean or wash as compared to others.

Adalaide Mentor

The only reason I started off staying away from sharing plastic and silicon utensils is because everyone in the house just loves to leave them all sitting in pans on the stove. Every spoon in the house is melty on the end which gives gluten all sorts of fun hiding places. I went with stainless steel pans and mostly metal utensils because even if someone else grabs mine they can't be ruined. If the only person you have to worry about is your husband and he's sensitive to your needs then I wouldn't be worried about plastic.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,218
    • Most Online (within 30 mins)
      7,748

    MCAyr
    Newest Member
    MCAyr
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      That should answer your question about gluten.  Plus a dermatitis herpetiformis diagnosis is definative of celiac disease by itself.  Now you need to decide if you need to to pursue a diagnosis.  For your baby's health, I would assune both you and the baby have Celiac Disease. Eat gluten free and account for the fact that gluten free foods are not fortified.  Make sure to get lots of folate and Choline to prevent neurotube defects.   My son was diagnosed when he was weaned by biopsy in 1976.  Everyone called it just colicky, but his giant abdomen and green and yellow poop said otherwise.  Oh, and dispite general belief, they do not outgrow it.  If you are gluten free then your newborn will be gluten free and testing will not be positive for celiac disease, until the baby starts eating gluten and gets sick.  Why put him through that?  Gluten free household will give him the best health. Just before I started gluten free and one of the reasons I did was that I was lying in bed watching TV when I coughed.  My belly was bloated and I felt sick as a dog.  A bubble, looked like Bazooka bubble gum, popped out of my navel.  I am male, but apparently umbilical hernias are not uncommon in pregnancy.  Mine eventually resolved by itself. Low choline levels in pregnant women raise babies' risk for brain and spinal-cord defects, study shows  "From 180,000 pregnant women screened between 2003 and 2005, the researchers identified 80 whose pregnancies were affected by neural tube defects. Choline, an essential nutrient found in egg yolks, soy, wheat germ and meats, was the only nutrient measured whose blood levels were linked to risk of neural tube defects."  
    • MCAyr
      Appreciate the comment thanks yes seems my doc wants to go down the skin biopsy route for dermatitis herpetiformis as don't need to be on gluten-free apparently but we shall see what they say. 
    • trents
      Welcome to the community @MCAyr! One thing you need to know is that in order for celiac disease diagnostic testing to be valid, you must not have been on a gluten-free diet already. The first stage of celiac disease testing involves looking for the blood antibodies that are produced by the inflammation in the small bowel lining. Once you eliminate gluten, the antibodies begin to disappear and it takes weeks or months of being back on normal amounts of gluten for them to build up to detectable levels again.
    • MCAyr
      Hi currently being investigated for celiac; suspected dermatitis herpetiformis, low calcium and vit D, stomach discomfort and 2 episodes of awful stomach pain (docs think maybe triggered by pregnancy)  Went gluten-free for 5 weeks was feeling great then last week accidentally had some in a sweet! Followed by 2 days of absolute hell and excruciating stomach pain and cramping below right of belly button. Since then the really bad pain has gone, but I've had sore to touch above my belly button and think I can feel a lump, was painful for a couple of days to point I couldn't sleep on sides. Docs palpated few days before I could feel lump, and felt nothing.  Anyone had a hernia they didn't know about until their gluten reaction inflamed it? Or is this just another lovely gluten sensitivity symptom?  Many thanks 
    • Scott Adams
      Your story is a powerful and heartbreaking testament to the profound damage that can be caused by undiagnosed celiac disease and the profound pain of not being believed or supported by family. It is sadly a common narrative within the celiac community to have suffered for years, even decades, while autoimmune conditions stack up, all while being dismissed. To answer your core question: yes, living in a environment with significant, constant gluten exposure, especially from airborne flour in a home where milling and baking occurred, would have created a perpetual state of autoimmune activation for you, even beyond the direct ingestion. This chronic exposure is strongly linked to the development and exacerbation of the very autoimmune disorders you describe—Migraines, Meniere's, Hashimoto's, and more. Your body was under constant attack, and the lack of care and understanding from your family compound that trauma significantly. It is not your fault. Many in the community share similar stories of a cascade of illnesses finally explained by a celiac diagnosis, often coming too late to prevent irreversible damage. While I cannot speak to the legal aspects of your inheritance situation, your experience with the medical neglect and the lasting impact of your childhood environment is deeply valid and shared by others who understand this unique type of suffering. Thank you for having the courage to share your truth. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
×
×
  • Create New...